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Advisor(s)
Abstract(s)
Reaction of N-acetylpyrazine-2-carbohydrazide (H2L) with anhydrous Fe(II) or Fe(III) chloride in CH3CN or in MeOH leads to the mononuclear [Fe(kNN’O-HL)Cl2] (1) or binuclear [Fe(kNN’O-HL) Cl(μ-OMe)]2 (2) Fe(III) complex, respectively. These complexes are characterized by elemental analysis, ESI-MS, IR spectroscopy, single-crystal X-ray crystallography, electrochemical techniques and DFT calculations. The theoretical calculations indicate that the three single-electron sequential reductions of 1 are centred at the metal, at the pyrazine group and at both, respectively. The catalytic activity of 1 and 2 was screened towards Friedel-Crafts benzoylation and acylation of m-xylene. The effects of reaction parameters, such as catalyst amount, reaction time and temperature, were studied and, under optimal conditions, 96% yield of 2,4-dimethylbenzophenone and 20% yield of 2,4-dimethylacetophenone were obtained, respectively. Complex 1 exhibited the highest activity in both reactions. The structural and electrochemical properties were supported by theoretical calculations and the importance of the Lewis acid character of the catalyst in the promotion of this catalytic reaction is discussed.
Description
Keywords
Benzoylation Fe(III) complexes Friedel-Crafts Reação de benzoilação Complexos de ferro
Citation
BARMAN, Tannistha Roy; [et al] – Efficient solvent-free friedel-crafts benzoylation and acylation of m-xylene catalyzed by N-acetylpyrazine-2-carbohydrazide-Fe(III)-chloro complexes. Chemistry Select. ISSN 2365-6549. Vol. 3, N.º 28 (2018), pp. 8349-8355
Publisher
Wiley-VCH Verlag